A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600062



Internal ID16387471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152145586hg38UCSC Ensembl
Innerchr5:151514956..151525147hg19UCSC Ensembl
Innerchr5:151495149..151505340hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3810192
hg1910192
hg1810192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10132n54
Supporting Variantsnssv1043973, nssv1043971, nssv1043972
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600062
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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